Coralgil

Coralgil

SCHEMBL317407

CCC(c1ccc(OCCN(CC)CC)cc1)C(CC)c1ccc(OCCN(CC)CC)cc1

nearest known ligand 0.64

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EBP Q15125 3/20 0.61
SIGMAR1 Q99720 3/20 0.61
CYP2D6 P10635 2/20 0.55
HTT P42858 2/20 0.55
CYP1A2 P05177 1/20 0.55
LTA4H P09960 1/20 0.55
CYP2C9 P11712 1/20 0.55
CYP2C19 P33261 1/20 0.55
ESR1 P03372 5/20 0.54
ESR2 Q92731 3/20 0.54
KDM4E B2RXH2 2/20 0.53
TSHR P16473 1/20 0.53
KMT2A Q03164 4/20 0.51
KCNH2 Q12809 2/20 0.51
CHRM2 P08172 2/20 0.51
ADRA2A P08913 2/20 0.51
ADORA3 P0DMS8 2/20 0.51
CHRM1 P11229 2/20 0.51
PTGS1 P23219 2/20 0.51
SLC6A2 P23975 2/20 0.51

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Coralgil SCHEMBL26128795 1.00 EBP (0.61) EBPSIGMAR1CYP2D6HTTCYP1A2
Coralgil SCHEMBL29989837 0.98 EBP (0.59) EBPSIGMAR1CYP2D6HTTCYP1A2
Coralgil SCHEMBL1649422 0.97 EBP (0.58) EBPSIGMAR1CYP2D6HTTCYP1A2
SCHEMBL9706125 0.85 EBP (0.72) EBPSIGMAR1CYP2D6HTTCYP1A2
SCHEMBL12015816 0.84 KDM4E (0.67) EBPSIGMAR1CYP2D6HTTCYP1A2
SCHEMBL2425061 0.81 EBP (0.55) EBPSIGMAR1CYP2D6HTTCYP1A2
SCHEMBL2426949 0.81 EBP (0.55) EBPSIGMAR1CYP2D6HTTCYP1A2
SCHEMBL9827594 0.81 EBP (0.59) EBPSIGMAR1CYP2D6HTTCYP1A2
SCHEMBL3420518 0.78 EBP (0.64) EBPSIGMAR1CYP2D6HTTCYP1A2
SCHEMBL864035 0.78 SLC2A1 (0.56) EBPSIGMAR1CYP2D6HTTCYP1A2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 178 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3485908-B1 THERAPEUTIC COMBINATION AND USE OF DLL4 ANTAGONIST ANTIBODIES AND ANTI-HYPERTENSIVE AGENTS MEREO BIOPHARMA 5 INC (US) 2021-08-18 EP claimed
EP-3072526-B1 THERAPEUTIC COMBINATION AND USE OF DLL4 ANTAGONIST ANTIBODIES AND ANTI-HYPERTENSIVE AGENTS ONCOMED PHARM INC (US) 2018-09-26 EP claimed
US-9511139-B2 Therapeutic combination and methods of treatment with a DLL4 antagonist and an anti-hypertensive agent ONCOMED PHARMACEUTICALS, INC. (US) 2016-12-06 US claimed
EP-3072526-A1 THERAPEUTIC COMBINATION AND USE OF DLL4 ANTAGONIST ANTIBODIES AND ANTI-HYPERTENSIVE AGENTS Oncomed Pharmaceuticals, Inc. (US) 2016-09-28 EP claimed
EP-2488204-B1 THERAPEUTIC COMBINATION AND USE OF DLL4 ANTAGONIST ANTIBODIES AND ANTI-HYPERTENSIVE AGENTS ONCOMED PHARM INC (US) 2016-04-06 EP claimed
US-20150118232-A1 Therapeutic Combination and Methods of Treatment With A DLL4 Antagonist and an Anti-Hypertensive Agent ONCOMED PHARMACEUTICALS, INC. 2015-04-30 US claimed
US-7354581-B2 Therapeutic combination of a VEGF antagonist and anti-hypertensive agent REGENERON PHARMACEUTICALS, INC. (US) 2008-04-08 US claimed
EP-1853298-A2 THERAPEUTIC COMBINATION OF A VEGF ANTAGONIST (VEGF TRAP) AND AN ANTI-HYPERTENSIVE AGENT REGENERON PHARMACEUTICALS, INC. (US) 2007-11-14 EP claimed
WO-2007098390-A2 METHOD FOR TREATING RESISTANT HYPERTENSION GILEAD COLORADO, INC. (US) 2007-08-30 WO claimed
WO-2006086544-A2 THERAPEUTIC COMBINATION OF A VEGF ANTAGONIST (VEGF TRAP) AND AN ANTI-HYPERTENSIVE AGENT REGENERON PHARMACEUTICALS, INC. (US) 2006-08-17 WO claimed
US-20060183684-A1 Therapeutic combination of a VEGF antagonist and anti-hypertensive agent REGENERON PHARMACEUTICALS, INC. 2006-08-17 US claimed
EP-1073470-A1 PHARMACEUTICAL COMPOSITIONS CONTAINING COMPOUNDS WITH ACTIVITY FOR THE ENHANCEMENT OF ABSORPTION OF ACTIVE INGREDIENTS INPHARMA S.A. (CH) 2001-02-07 EP claimed
WO-2000048636-A1 PHARMACEUTICAL COMPOSITIONS CONTAINING COMPOUNDS WITH ACTIVITY FOR THE ENHANCEMENT OF ABSORPTION OF ACTIVE INGREDIENTS INPHARMA S.A. (CH) 2000-08-24 WO claimed
US-20240374559-A1 COMPOSITION COMPRISING PPAR-MODULATOR AND AN UROLITHIN DERIVATIVE AND USES THEREOF INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE - INSERM (FR) 2024-11-14 US disclosed
US-20240293358-A1 COMPOSITION COMPRISING PPAR-MODULATOR AND AN UROLITHIN DERIVATIVE AND USES THEREOF Universite de Bordeaux (FR) 2024-09-05 US disclosed
EP-4333827-A1 COMPOSITION COMPRISING PPAR-MODULATOR AND AN UROLITHIN DERIVATIVE AND USES THEREOF UNIVERSITE DE BORDEAUX (FR) 2024-03-13 EP disclosed
US-5446070-A Flexible, finite, bioadhesive, therapeutical agent in solid form NOVER PHARMACEUTICALS, INC. (US) 1995-08-29 US disclosed
EP-0449463-B1 Method and composition for iontophoresis BECTON DICKINSON CO (US) 1994-11-30 EP disclosed
US-5302172-A Method and composition for iontophoresis NORTH CAROLINA STATE UNIVERSITY (US) 1994-04-12 US disclosed
EP-0449463-A2 Method and composition for iontophoresis Becton, Dickinson and Company (US) 1991-10-02 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20240293358-A1 COMPOSITION COMPRISING PPAR-MODULATOR AND AN UROLITHIN DERIVATIVE AND USES THEREOF PPARD, PPARA, PPARG EBP 785/4885SIGMAR1 2201/4885CYP2D6 2553/4885
US-20240374559-A1 COMPOSITION COMPRISING PPAR-MODULATOR AND AN UROLITHIN DERIVATIVE AND USES THEREOF PPARD, PPARA, PPARG EBP 785/4885SIGMAR1 2201/4885CYP2D6 2553/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.